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HS Code |
906823 |
| Chemicalname | 4-N-Hexyloxybromobenzene |
| Casnumber | 57260-69-6 |
| Molecularformula | C12H17BrO |
| Molecularweight | 257.17 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 346.9 °C at 760 mmHg |
| Density | 1.22 g/cm3 |
| Refractiveindex | 1.524 |
| Solubility | Insoluble in water, soluble in organic solvents |
| Flashpoint | 163.3 °C |
| Smiles | CCCCCCOC1=CC=C(C=C1)Br |
As an accredited 4-N-Hexyloxybromobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a secure screw cap, labeled "4-N-Hexyloxybromobenzene," hazard symbols, and handling instructions. |
| Shipping | 4-N-Hexyloxybromobenzene is shipped in tightly sealed containers, protected from light and moisture. It should be transported following all local, national, and international regulations for hazardous substances. The package must be clearly labeled, handled with care, and kept in a cool, dry place, away from incompatible materials. |
| Storage | 4-N-Hexyloxybromobenzene should be stored in a tightly sealed container, protected from light, heat, and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Label the container clearly and store at room temperature unless otherwise specified. Ensure the storage area is equipped for the safe handling of hazardous chemicals. |
Applications of 4-N-Hexyloxybromobenzene in Industrial ManufacturingAs a manufacturer specializing in aromatic intermediates, we produce 4-N-Hexyloxybromobenzene for a range of advanced chemical applications. Below, we detail its industrial uses, relevant compliance requirements, formulation approaches, integration points, and typical downstream goods. 1. Liquid Crystal Intermediates for Display MaterialsAdvanced liquid crystal display (LCD) panel production relies on high-purity aromatic intermediates during synthesis of mesogenic compounds. This brominated ether functions as a precision reactant in Suzuki, Heck, or Ullmann-type couplings for the construction of terminal and side-chain substituted liquid crystal cores. Digital device manufacturers require stringent quality assurance in each batch to secure stable phase behavior and electro-optical performance throughout production. Industry compliance standards
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2. Organic Synthesis for Pharmaceutical IntermediatesMedicinal chemistry and contract synthesis operations use this compound as a building block for advanced pharmaceutical intermediates. It supports the synthesis of molecules with aryl-ether linkages, especially where a hexyloxy chain confers improved solubility or metabolic stability in the drug candidate. The bromine substituent enables site-selective cross-coupling for efficient SAR (Structure–Activity Relationship) explorations. Industry compliance standards
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3. High-Performance Polymers for Specialty CoatingsIn high-value polymer chemistry, brominated aromatic ethers can initiate controlled side-chain modifications in poly(aryl ether) matrices. This raw material introduces hexyloxy substituents that enhance flexibility, surface hydrophobicity, and dielectric properties, vital for coatings in electronics and specialty engineering applications demanding consistent insulation and low surface tension under exposure to environmental stresses. Industry compliance standards
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4. Performance Additives for Advanced Lubricant FormulationsChemical formulators for industrial lubrication systems utilize functionalized aryl ethers to impart desirable solubility or viscosity-control properties in high-end synthetic lubricants. The hexyloxy functionality enhances compatibility with synthetic base oils, while the aromatic core enables fine-tuning of oxidative stability and thermal endurance in specialty lube systems. Industry compliance standards
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5. Organic Electronics – Precursors for Conductive PolymersManufacturers focusing on organic electronic materials employ this compound for synthesizing key building blocks in semiconductive polymers. The structure supports selective cross-coupling to generate flexible, soluble polymer backbones, crucial for maximizing hole mobility and maintaining solution processability in printed electronics fabrication. Industry compliance standards
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